Align Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized)
to candidate WP_038857748.1 AFK65_RS05695 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC
Query= TCDB::Q72L52 (376 letters) >NCBI__GCF_001277175.1:WP_038857748.1 Length = 371 Score = 335 bits (859), Expect = 1e-96 Identities = 187/361 (51%), Positives = 243/361 (67%), Gaps = 9/361 (2%) Query: 1 MAKVRLEHVWKRFGK-VVAVKDFNLETEDGEFVVFVGPSGCGKTTTLRMIAGLEEISEGN 59 MA++RLE V KR+G +K +L+ GEFVV VGPSGCGK+T LR++AGLEEI++G+ Sbjct: 1 MAQLRLEKVQKRYGTHAEVIKPLDLQINSGEFVVVVGPSGCGKSTLLRLVAGLEEITDGD 60 Query: 60 IYIGDRLVNDVPPKDRDIAMVFQNYALYPHMNVYENMAFGLRLRRYPKDEIDRRVKEAAR 119 +YI D+ VND P +R I MVFQ+YALYPHM VY+NMAF L + + P+ EID RV+E+AR Sbjct: 61 MYIDDQRVNDDSPSERGIGMVFQSYALYPHMTVYQNMAFALEMAKVPEKEIDERVRESAR 120 Query: 120 ILKIEHLLNRKPRELSGGQRQRVAMGRAIVREPKVFLMDEPLSNLDAKLRVEMRAEIAKL 179 IL++EHLL+R+P++LSGGQRQRVA+GRAIVREP +FL DEPLSNLDA LRV+MR EIA L Sbjct: 121 ILQLEHLLDRRPKDLSGGQRQRVAIGRAIVREPSLFLFDEPLSNLDASLRVQMRMEIAAL 180 Query: 180 QRRLGVTTIYVTHDQVEAMTLGHRIVVMKDGEIQQVDTPLNLYDFPANRFVAGFIGSPSM 239 RR+ T +YVTHDQVEAMTL RIVV+ G+I+QV TPL LYD PAN FVA FIGSP M Sbjct: 181 HRRIHATILYVTHDQVEAMTLADRIVVLNQGQIEQVGTPLALYDTPANVFVAQFIGSPKM 240 Query: 240 NFVRAGVEVQGEKVYLVAPGFRIRANAVLGSALKPYAGKEVWLGVRPEHLGLKGYTTIPE 299 N + + E V +R + A+ G V LG+RPEH+ + T+ + Sbjct: 241 NLIPGKMLRVMEHACEVELENGLRLTLPV-QAVAGQEGDAVQLGIRPEHVEI---MTLAK 296 Query: 300 EENVLRGEVEVVEPLGAETEIHV--AVNGTLLVAKVDGHAPVKPGDKVELLADTQRLHAF 357 + + GEV VE +G ET ++V LV + V+P + L + + F Sbjct: 297 AD--VEGEVLFVEHMGNETLVYVNGGYGAEPLVMRHTERLEVRPEHHLGLKLPAEHCYLF 354 Query: 358 D 358 D Sbjct: 355 D 355 Lambda K H 0.320 0.139 0.400 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 467 Number of extensions: 28 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 376 Length of database: 371 Length adjustment: 30 Effective length of query: 346 Effective length of database: 341 Effective search space: 117986 Effective search space used: 117986 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory